Page last updated: 2024-12-05

dimethyl phosphate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Dimethyl phosphate (DMP) is a colorless, odorless liquid with a high boiling point. It is a highly reactive and versatile compound commonly used in organic synthesis as a phosphorylating agent. DMP can be synthesized by the reaction of phosphorus oxychloride (POCl3) with methanol in the presence of a base. It has been used in the synthesis of various pharmaceuticals, pesticides, and other industrial chemicals. DMP is also a key component in the biosynthesis of DNA and RNA, where it serves as a phosphate donor. Its importance lies in its ability to transfer phosphate groups to other molecules, playing a crucial role in cellular processes like energy metabolism and signal transduction. Research into DMP often focuses on its applications in organic synthesis, its role in biological systems, and its potential environmental impact.'

dimethyl phosphate: excreted in urine after exposure to mevinphos; RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID13134
CHEBI ID166474
SCHEMBL ID47754
MeSH IDM0050703

Synonyms (42)

Synonym
unii-hi4k2c9uei
hi4k2c9uei ,
4-01-00-01259 (beilstein handbook reference)
CHEBI:166474
dimethyl hydrogen phosphate
813-78-5
nsc2676
methyl phosphate ((meo)2(ho)po)
phosphoric acid, dimethyl ester
dimethyl phosphate
o,o-dimethyl phosphate
nsc-2676
nsc-289396
nsc289396
53396-59-1
nsc 2676
einecs 212-389-6
brn 1702242
ai3-15058
o,o-dimethyl hydrogen phosphate
dimethylphosphate
tox21_301411
NCGC00255372-01
cas-813-78-5
dtxsid5025150 ,
dtxcid205150
AKOS015965163
dimethoxyphosphinic acid
BP-21444
SCHEMBL47754
mfcd00014887
dimethyl phosphate, aldrichcpr
BBL102569
STL556372
Q2823255
dimethyl phosphoric acid
kfg ,
phosphoric acid dimethyl ester
dimethylhydrogenphosphate
dimethyl phosphate (olaparib impurity)
CS-0164327
dimethylphosphate; phosphoric acid, dimethyl ester;

Research Excerpts

Overview

Dimethyl phosphate (DMP) is a metabolite of phosphamidon, mevinphos, dicrotophos, monocrotophos and dichlorvos.

ExcerptReferenceRelevance
"Dimethyl phosphate (DMP) is a metabolite of phosphamidon, mevinphos, dicrotophos, monocrotophos, dichlorvos, and trichlorfon."( Acute poisoning with phosphamidon: determination of dimethyl phosphate (DMP) as a stable metabolite in a case of organophosphate insecticide intoxication.
Daldrup, T; Kardel, B; Pier, S; Tarbah, FA; Temme, O, 2004
)
1.3

Toxicity

ExcerptReferenceRelevance
" Results of our study has proved the negative impact of ILs on the tested plants and the toxic effect of imidazolium salts was dependent primarily on the applied ionic liquids concentration."( The role of the anion in the toxicity of imidazolium ionic liquids.
Bałczewski, P; Biczak, R; Pawłowska, B; Rychter, P, 2014
)
0.4

Dosage Studied

ExcerptRelevanceReference
" A dose-response relationship was found between urinary concentrations of DMP and ADHD in both crude and adjusted analyses (p for trend<0."( Increased risk of attention-deficit/hyperactivity disorder associated with exposure to organophosphate pesticide in Taiwanese children.
Chen, ML; Chen, YS; Chien, LC; Chiou, HC; Chung, MY; Du, JC; Fuh, MR; Hwang, B; Yang, W; Yu, CJ, 2016
)
0.43
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
dialkyl phosphate
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (1)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency0.25210.001530.607315,848.9004AID1224841
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (90)

TimeframeStudies, This Drug (%)All Drugs %
pre-199015 (16.67)18.7374
1990's8 (8.89)18.2507
2000's21 (23.33)29.6817
2010's38 (42.22)24.3611
2020's8 (8.89)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 43.68

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index43.68 (24.57)
Research Supply Index4.57 (2.92)
Research Growth Index4.90 (4.65)
Search Engine Demand Index64.13 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (43.68)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (1.05%)5.53%
Reviews1 (1.05%)6.00%
Case Studies1 (1.05%)4.05%
Observational1 (1.05%)0.25%
Other91 (95.79%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]